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L Mandel

Showing results (311-320 of 451) with videos related to

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Nucleic Acids Research|February 11, 1989
A probe from an X-Y homology region detects RFLPs in Xq13-q22R P Feil, E Gillard, N A Affara, et al.
American Journal of Human Genetics|June 1, 1997
A mutation in the MTM1 gene invalidates a previous suggestion of nonallelic heterogeneity in X-linked myotubular myopathyC Guiraud-Chaumeil, M C Vincent, J Laporte, et al.
Human Molecular Genetics|August 7, 2001
SCA7 mouse models show selective stabilization of mutant ataxin-7 and similar cellular responses in different neuronal cell typesG Yvert, K S Lindenberg, D Devys, et al.
Human Genetics|September 1, 1987
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27I Oberlé, G Camerino, K Wrogemann, et al.
Organic Letters|October 18, 2012
Structure of FD-895 revealed through total synthesisReymundo Villa, Alexander L Mandel, Brian D Jones, et al.
Plos One|October 23, 2010
Individual differences in AMY1 gene copy number, salivary α-amylase levels, and the perception of oral starchAbigail L Mandel, Catherine Peyrot des Gachons, Kimberly L Plank, et al.
Archives of Internal Medicine|April 14, 2004
Patients' interest in reading their medical record: relation with clinical and sociodemographic characteristics and patients' approach to health careJinnet B Fowles, Allan C Kind, Cheryl Craft, et al.
Lancet (London, England)|May 5, 1990
Prenatal diagnosis of Friedreich ataxiaA Hanauer, R Fujita, P Trouillas, et al.
American Journal of Medical Genetics|April 1, 1992
Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic associationI Oberlé, J Boué, M F Croquette, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994H F Willard, F Cremers, J L Mandel, et al.
Pageof 46

Showing results (311-320 of 451) with videos related to

Sort By:
Pageof 46
Nucleic Acids Research|February 11, 1989
A probe from an X-Y homology region detects RFLPs in Xq13-q22R P Feil, E Gillard, N A Affara, et al.
American Journal of Human Genetics|June 1, 1997
A mutation in the MTM1 gene invalidates a previous suggestion of nonallelic heterogeneity in X-linked myotubular myopathyC Guiraud-Chaumeil, M C Vincent, J Laporte, et al.
Human Molecular Genetics|August 7, 2001
SCA7 mouse models show selective stabilization of mutant ataxin-7 and similar cellular responses in different neuronal cell typesG Yvert, K S Lindenberg, D Devys, et al.
Human Genetics|September 1, 1987
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27I Oberlé, G Camerino, K Wrogemann, et al.
Organic Letters|October 18, 2012
Structure of FD-895 revealed through total synthesisReymundo Villa, Alexander L Mandel, Brian D Jones, et al.
Plos One|October 23, 2010
Individual differences in AMY1 gene copy number, salivary α-amylase levels, and the perception of oral starchAbigail L Mandel, Catherine Peyrot des Gachons, Kimberly L Plank, et al.
Archives of Internal Medicine|April 14, 2004
Patients' interest in reading their medical record: relation with clinical and sociodemographic characteristics and patients' approach to health careJinnet B Fowles, Allan C Kind, Cheryl Craft, et al.
Lancet (London, England)|May 5, 1990
Prenatal diagnosis of Friedreich ataxiaA Hanauer, R Fujita, P Trouillas, et al.
American Journal of Medical Genetics|April 1, 1992
Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic associationI Oberlé, J Boué, M F Croquette, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994H F Willard, F Cremers, J L Mandel, et al.
Pageof 46